High-Efficiency Deep-Red Light-Emitting Electrochemical Cell Based on a Trinuclear Ruthenium(II)-Silver(I) Complex.
Babak Nemati BidehHashem ShahroosvandMohammad Kahaj Khaja NazeeruddinPublished in: Inorganic chemistry (2021)
Turn-on time is a key factor for lighting devices to be of practical application. To decrease the turn-on time value of a deep-red light-emitting electrochemical cells (DR-LECs), two novel approaches based on molecularly engineered ruthenium phenanthroimidazole complexes were introduced. First, we found that with the incorporation of ionic methylpyridinium group to phenanthroimidazole ligand, the turn-on time of the DR-LECs device was dramatically reduced, from 79 to 27 s. By complexation of ruthenium emitter with Ag+, the turn-on time was improved by 85%, and the EQE of DR-device was increased from 0.62 to 0.71%. These results open a new avenue in decreasing the turn-on time without adding ionic electrolytes, leading to an efficient LEC.
Keyphrases
- light emitting
- fluorescent probe
- living cells
- ionic liquid
- sensitive detection
- gold nanoparticles
- high efficiency
- editorial comment
- quantum dots
- induced apoptosis
- single cell
- minimally invasive
- cell therapy
- cell cycle arrest
- signaling pathway
- oxidative stress
- cell death
- cell proliferation
- endoplasmic reticulum stress
- mesenchymal stem cells
- solid phase extraction
- visible light